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| Structural eye disease v0.91 | FKTN | Nicola Ragge reviewed gene: FKTN: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.89 | FKTN |
Ivone Leong Source Expert Review Green was added to FKTN. Source NHS GMS was added to FKTN. Rating Changed from Amber List (moderate evidence) to Green List (high evidence) |
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| Structural eye disease v0.88 | FKTN |
Ivone Leong Source Expert Review Amber was added to FKTN. Rating Changed from Red List (low evidence) to Amber List (moderate evidence) |
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| Structural eye disease v0.60 | FKTN | Mariya Moosajee reviewed gene: FKTN: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Muscular Dystrophy-Dystroglycanopathy, Type A, 4, MDDGA4; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.59 | FKTN |
Ivone Leong gene: FKTN was added gene: FKTN was added to Structural eye disease. Sources: London North GLH Mode of inheritance for gene: FKTN was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: FKTN were set to Muscular Dystrophy-Dystroglycanopathy, Type A, 4, MDDGA4, 253800 |
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